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利用多学科监督委员会确保退伍军人事务部卫生系统符合 USP<797>和<800>。

Leveraging a multidisciplinary oversight committee to ensure USP <797> and <800> compliance at a Veterans Affairs health system.

机构信息

Department of Pharmacy, VA Palo Alto Health Care System, Palo Alto, CA, USA.

出版信息

Am J Health Syst Pharm. 2022 Feb 8;79(4):276-282. doi: 10.1093/ajhp/zxab412.

Abstract

PURPOSE

Producing compounded sterile preparations (CSP) of the highest quality and ensuring safe hazardous drug handling are well-established priorities for pharmacy departments. Maintaining compliance with United States Pharmacopeia general chapters 797 and 800 (USP <797> and <800>) must also be a priority for health-system leadership. This report describes how a pharmacy-driven multidisciplinary committee was created to provide USP <797> and <800> oversight within a multicampus Veterans Affairs health system and the facility and safety outcomes achieved.

SUMMARY

The Veterans Health Administration required facilities to establish an oversight committee to ensure USP-compliant CSP procedures and the safe handling of hazardous drugs in all aspects of the medication-use process. Spearheaded by the pharmacy department, the VA Palo Alto Health Care System (VAPAHCS) chartered the CSP Advisory Committee to achieve this goal.The membership was composed of department heads in the areas of pharmacy, nursing, environmental management services, engineering, facility planning, safety, industrial hygiene, employee health, supply chain services, infection control, and quality management and the health system's director's office. The medication safety officer served as the executive secretary for the advisory committee and was responsible for agenda development, minutes, and coordinating timely follow-ups on action items; the VAPAHCS deputy director served as chair. Monthly meetings were conducted to receive updates on targeted sterile compounding and hazardous drug handling objectives: environmental controls and monitoring, compliance with regulatory requirements, staff competency, hazardous drug exposure event analyses, and development of well-defined health-system policy to guide practice.

CONCLUSION

Taking a multidisciplinary approach to USP <797> and <800> compliance facilitated communications, created engagement, and ensured completion of action plans.

摘要

目的

生产最高质量的复合无菌制剂(CSP)并确保安全处理危险药物,这是药剂科的既定优先事项。遵守美国药典通则 797 和 800(USP <797> 和 <800>)也是医疗系统领导层的首要任务。本报告介绍了如何创建一个由药剂科主导的多学科委员会,以提供 USP <797> 和 <800> 的监督,这是在一个多校区退伍军人事务医疗系统内进行的,还介绍了所实现的设施和安全成果。

摘要

退伍军人事务管理局要求各设施建立监督委员会,以确保符合 USP 的 CSP 程序以及在用药过程的各个方面安全处理危险药物。由药剂科牵头,VA 帕洛阿尔托医疗保健系统(VAPAHCS)成立了 CSP 咨询委员会来实现这一目标。委员会成员包括药剂、护理、环境管理服务、工程、设施规划、安全、工业卫生、员工健康、供应链服务、感染控制和质量管理以及医疗系统主任办公室等部门的负责人。用药安全官员担任咨询委员会的执行秘书,负责制定议程、记录会议纪要,并协调及时跟进行动项目;VAPAHCS 副主任担任主席。每月举行会议,以了解以下目标的最新进展:靶向无菌复合和危险药物处理、环境控制和监测、法规要求的遵守、员工能力、危险药物暴露事件分析以及制定明确的卫生系统政策以指导实践。

结论

采用多学科方法遵守 USP <797> 和 <800> 有助于沟通、激发参与度,并确保行动计划的完成。

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